Canonical Allele Identifier: PA2826567338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182967
ClinVar RCV Id: RCV000161070 RCV003621508 RCV004019947 RCV004019946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ile212Ser
CA000396
NM_001276761.3:c.635T>G